A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3673934



Internal ID18972215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144220496..144391466hg38UCSC Ensembl
Innerchr7:143917589..144088559hg19UCSC Ensembl
Innerchr7:143548522..143719492hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38170971
hg19170971
hg18170971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024851
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3673934
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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